Please use this identifier to cite or link to this item: https://doi.org/10.1186/s13000-017-0643-2
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dc.titleHeterotopic pancreas in the omphalomesenteric duct remnant in a 9-month-old girl: A case report and literature review
dc.contributor.authorZhao, Z
dc.contributor.authorSim, C.K
dc.contributor.authorMantoo, S
dc.date.accessioned2020-10-23T04:43:03Z
dc.date.available2020-10-23T04:43:03Z
dc.date.issued2017
dc.identifier.citationZhao, Z, Sim, C.K, Mantoo, S (2017). Heterotopic pancreas in the omphalomesenteric duct remnant in a 9-month-old girl: A case report and literature review. Diagnostic Pathology 12 (1) : 49. ScholarBank@NUS Repository. https://doi.org/10.1186/s13000-017-0643-2
dc.identifier.issn17461596
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179476
dc.description.abstractBackground: Heterotopic pancreas most commonly occurs in the upper gastrointestinal tract of adults, usually as an incidental finding. It seldom occurs at the umbilicus, and even rarely in the pediatric age group. Case presentation: Here we present a case of heterotopic pancreatic tissue in the omphalomesenteric duct remnant of a 9-month-old baby girl. She presented with redness at the base of the umbilicus associated with occasional mild wetness. A urachal fistula was suspected by ultrasound. Histology from subsequent resection revealed fibrous tissue with heterotopic pancreatic tissue and accompanying small bowel mucosa. The patient's umbilical redness resolved after the surgery. Conclusions: Upon literature search, we found only 17 other cases of heterotopic pancreas reported in the umbilicus. They described a high male to female ratio, frequent association with omphalomesenteric duct remnant and presentation of umbilical discharge. The Heinrich system is frequently used to classify heterotopic pancreas into 3 types, based on the presence of acini, islets and ducts. Several mechanisms have been proposed on the pathogenesis of heterotopic pancreas, including misplacement, metaplasia and totipotent cell theories. Heterotopic pancreas can manifest clinically with diseases of the pancreas, including malignant transformation, reported as high as 12.7% in a series. Awareness of this finding in the biopsy aids the suitable treatment decisions for the patient. @ 2017 The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcase report
dc.subjectchoristoma
dc.subjectdiagnostic imaging
dc.subjectfemale
dc.subjecthuman
dc.subjectincidental finding
dc.subjectinfant
dc.subjectintestine mucosa
dc.subjectpancreas disease
dc.subjectpathology
dc.subjectsmall intestine
dc.subjectumbilicus
dc.subjectvitelline duct
dc.subjectChoristoma
dc.subjectFemale
dc.subjectHumans
dc.subjectIncidental Findings
dc.subjectInfant
dc.subjectIntestinal Mucosa
dc.subjectIntestine, Small
dc.subjectPancreatic Diseases
dc.subjectUmbilicus
dc.subjectVitelline Duct
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s13000-017-0643-2
dc.description.sourcetitleDiagnostic Pathology
dc.description.volume12
dc.description.issue1
dc.description.page49
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